Islam A F M Fakhrul, Walkden-Brown Stephen W, Islam Aminul, Underwood Gregory J, Groves Peter J
Centre for Animal Health and Welfare, School of Rural Science and Agriculture, The University of New England, Armidale, NSW, 2351, Australia.
Avian Pathol. 2006 Feb;35(1):42-8. doi: 10.1080/03079450500465734.
Vaccination with herpesvirus of turkey (HVT) vaccine provides protection against clinical Marek's disease (MD) but does not preclude infection with wild-type MD virus (MDV). The quantity of MDV detected in circulating lymphocytes during the early period after infection may be a useful predictor of subsequent clinical MD later in the life. A study was designed to quantify MDV and HVT copy number in peripheral blood lymphocytes (PBL) using real-time polymerase chain reaction between days 5 and 35 post-challenge and to relate this to subsequent development of gross MD lesions. Female commercial broiler chickens were vaccinated with HVT or were sham-vaccinated at hatch, then challenged with MDV strain MPF-57 at day 2 post-vaccination and reared in positive-pressure isolators up to 56 days post-challenge, when all survivors were euthanized. All dead and euthanized chickens were examined post mortem for gross MD lesions. Birds were scored for MD lesions and mortality. MDV and HVT genome copy numbers were determined for each PBL sample. There was an increase in HVT load in PBL between days 7 and 37 post-vaccination, with marked increases between days 7 and 16 and again between days 30 and 37. There was a steady increase in MDV load to 35 days post-challenge. The mean MDV copy number (log(10)) was greater in chickens subsequently exhibiting gross MD lesions (5.05 +/- 0.21) than in those that did not (2.88 +/- 0.223), with the largest difference at 14 and 21 days post-challenge (P < 0.001). Quantification of MDV during early infection is therefore a potential tool for monitoring MD in broiler flocks.
接种火鸡疱疹病毒(HVT)疫苗可预防临床马立克氏病(MD),但不能排除感染野生型MD病毒(MDV)。感染后早期在循环淋巴细胞中检测到的MDV数量可能是鸡后期临床MD的有用预测指标。本研究旨在通过实时聚合酶链反应定量攻毒后第5天至第35天外周血淋巴细胞(PBL)中的MDV和HVT拷贝数,并将其与随后大体MD病变的发展相关联。雌性商品肉鸡在孵化时接种HVT或进行假接种,然后在接种后第2天用MDV毒株MPF-57攻毒,并在正压隔离器中饲养至攻毒后56天,此时所有存活鸡均实施安乐死。对所有死亡和安乐死的鸡进行尸检以检查大体MD病变。对鸡的MD病变和死亡率进行评分。测定每个PBL样本的MDV和HVT基因组拷贝数。接种后第7天至第37天PBL中的HVT载量增加,在第7天至第16天以及第30天至第37天显著增加。攻毒后至第35天MDV载量稳步增加。随后出现大体MD病变的鸡的平均MDV拷贝数(log(10))(5.05±0.21)高于未出现病变的鸡(2.88±0.223),在攻毒后第14天和第21天差异最大(P<0.001)。因此,早期感染期间MDV的定量是监测肉鸡群MD的潜在工具。